Supplier Quality Engineer

PayCruit

Bedford (MA)

On-site

USD 110,000 - 140,000

Full time

7 days ago
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Job summary

PayCruit is seeking a Sr. Supplier Quality Engineer in Bedford, MA to lead process validation and supplier qualification programs for a broad parts portfolio.

You will partner with R&D, design, and production teams to prevent defects and drive supplier performance improvements across plastics, metals, and electronics. The ideal candidate has a 3+ year engineering background in manufacturing or product quality, knowledge of APQP, PFMEA, and CTS/CTQ criteria, and a track record of problem solving

Qualifications

  • Bachelor's degree in engineering; Master preferred.
  • 3+ years engineering experience in manufacturing or product quality.
  • Experience in process validation and verification (IQ/OQ/PQ).
  • SO 13485 Lead Auditor certification is a plus.
  • Experience with plastics, metal, and electronics.

Responsibilities

  • Perform Process Validation and Verification across Spectrawave IGTD portfolios for Consoles and Catheter parts.
  • Collaborate with R&D and Quality Design Assurance in Design for Manufacturability and Part Risk management per DFMAE and PFMEA.
  • Perform Process Validation , Verification, Test Method Validation, and assess CTS/CTQ criteria per APQP requirement for +700 parts.
  • Support Supplier Qualification including Audit, Quality Agreement and Change Notice Agreement.
  • Perform Problem solving in the case of FAI and APQP failure.
  • Deep dive Value Stream mapping across process.
  • Conducts thorough investigations of defects to determine if they are supplier-caused and implement corrections using the SCAR process.
  • Proactively manage, monitor, and troubleshoot supplier-related issues for quality of components, sub-assemblies, and assemblies including monitoring trends and managing Supplier Improvement and Supplier Quality Performance Monitoring.
  • Providing Quality oversight of product/process change requests from suppliers (SICRs: Supplier Initiated Chage Requests), ensuring appropriate regulatory review and adequate validation to support requested changes including following our APQP process and leading process validation, as necessary.
  • Develop and oversee process validation plans, including equipment qualifications, with suppliers and lead continuous improvement projects based on process/product trends, customer complaints, industry standards and government regulations.

Skills

Process Validation
APQP
Supplier Quality
Problem Solving
Cross-functional collaboration

Education

Bachelor's degree in Engineering
Master's degree preferred

Job description

Job Title: Sr. Supplier Quality Engineer

Job Location: Bedford MA

Job Duration: 12+ Months Contract

Description:

Local candidates to the Bedford MA preferred. Colorado Springs or Plymouth, MN are options.

Notes from the manager:

Major focus in experienced Process Validation, Verification across plastic, metal and electronics along with problem solving for candidates to support +700 parts for part qualification for Spectrawave products. The product contains Catheter and Console (System) products. Manufacture engineering, Product Quality, and/or SQE with this hands-on experience in Process Validation, Verification and TMV (Test Method Validation) would be right fit to this role.

Sr. Supplier Quality Engineer

In this role you

Responsible for achieving a state of high-quality performance at our Supplier partners through the application and practice of Advanced Product Quality Planning ‘APQP’ , Supplier Qualification (Audit, Quality Agreement/Change Notice Agreement), and continuous monitoring the performance supplier to drive zero defect through Supplier Corrective Actions and notification. You will fill a high-profile, cross functional position and play an integral role enabling development and production flow of Client IGTD’s critical supply base. You will work in close coordination with Product Engineering, Supply Chain and Production and Suppliers to execute effective, creative and smart supply chain strategies to achieve production goals.

Your role:

Perform Process Validation and Verification across Spectrawave IGTD portfolios for Consoles and Catheter parts.

  • Collaborate with R&D and Quality Design Assurance in Design for Manufacturability and Part Risk management per DFMAE and PFMEA.
  • Perform Process Validation , Verification, Test Method Validation, and assess CTS/CTQ criteria per APQP requirement for +700 parts.
  • Support Supplier Qualification including Audit, Quality Agreement and Change Notice Agreement.
  • Perform Problem solving in the case of FAI and APQP failure.
  • Deep dive Value Stream mapping across process.
  • Conducts thorough investigations of defects to determine if they are supplier-caused and implement corrections using the SCAR process.
  • Proactively manage, monitor, and troubleshoot supplier-related issues for quality of components, sub-assemblies, and assemblies including monitoring trends and managing Supplier Improvement and Supplier Quality Performance Monitoring.
  • Providing Quality oversight of product/process change requests from suppliers (SICRs: Supplier Initiated Chage Requests), ensuring appropriate regulatory review and adequate validation to support requested changes including following our APQP process and leading process validation, as necessary.
  • Develop and oversee process validation plans, including equipment qualifications, with suppliers and lead continuous improvement projects based on process/product trends, customer complaints, industry standards and government regulations.
You're the right fit if:

Bachelor Degree engineering (Master Degree is plus). 3+ years of engineering experience (Manufacturing Engineer and/or Product Quality is plus).

In-depth product manufacturing and quality experience in process validation and verification

  • Subject Matter in IQ, OQ, PQ
  • SO 13485 Lead Auditor certified is plus.
  • Experienced in plastic , metal, electronics commodities.
  • Strong written, oral and interpersonal skills to be able to effectively interface interdepartmentally and complete assignments with accuracy and a high attention to detail
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